EUCTR2012-001496-36-AT进行中(未招募)1 期
Multiple-dose pharmacokinetics of ampicillin / sulbactam and amoxicillin / clavulanic acid during haemodialysis in longterm haemodialysis patients - AMPISUL/AMOXICLAV-HD_V1.4
Medizinische Universität Wien, Universitätsklinik für Innere Medizin I, Klinische abteilung für Infektionen und Tropenme0 个研究点目标入组 16 人开始时间: 2013年6月25日最近更新:
适应症
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 16
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •a)Age >18 years
- •b)Suspected or proven bacterial infection requiring parenteral antibiotic therapy.
- •c)Organ replacement therapy (HD)
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range 12
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range 4
排除标准
- •a)Known hypersensitivity to ampicillin / sulbactam, amoxicillin / clavulanic acid or other beta-lactames, or severe hypersensitivity (anaphylactic reaction) to beta-lactam antibacterial agents.
- •b)An expected survival of less than two days.
- •c)Known pregnancy
- •d)Co-administration of one of the following drugs:
- •-probenecid
- •which cannot be discontinued for the duration of the study
- •e)Ampicillin / sulbactam respectively amoxicillin / clavulanic acid as monotherapy for resistant species or fungal infections.
- •f)Other reasons opposing the study participation on the discretion of the investigators.
研究者
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